EP2877148A2 - Composition d'écran solaire, resistant a l'eau haute protection améliorée - Google Patents

Composition d'écran solaire, resistant a l'eau haute protection améliorée

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Publication number
EP2877148A2
EP2877148A2 EP13747962.2A EP13747962A EP2877148A2 EP 2877148 A2 EP2877148 A2 EP 2877148A2 EP 13747962 A EP13747962 A EP 13747962A EP 2877148 A2 EP2877148 A2 EP 2877148A2
Authority
EP
European Patent Office
Prior art keywords
range
sunscreen
composition according
sunscreen composition
less
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP13747962.2A
Other languages
German (de)
English (en)
Inventor
Lene BRITZE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Riemann Trading ApS
Original Assignee
Riemann Trading ApS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Riemann Trading ApS filed Critical Riemann Trading ApS
Publication of EP2877148A2 publication Critical patent/EP2877148A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8176—Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30—Characterized by the absence of a particular group of ingredients
    • A61K2800/31—Anhydrous
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/48—Thickener, Thickening system

Definitions

  • the present invention relates to sunscreen compositions.
  • the present invention relates to sunscreen compositions with reduced amounts of film forming polymers and high water resistance.
  • UV irradiation causes skin burns, loss of skin elasticity and the appearance of wrinkles, promoting premature skin aging.
  • UV irradiation promotes the triggering of the erythemal reaction or accentuates this reaction in certain individuals and may even be the source of phototoxic or photoallergy reactions.
  • Last, but not least important, UV irradiation has carcinogenic effects. For these reasons, continuous need exists for means for protecting the skin against the harmful effects of UV irradiation.
  • compositions are preferred which have a pleasant feel and are formulated as non-greasy sprays, milks and creams that are easily applied. It is further preferred that the compositions exhibit non-adherence to sand, as users of these compositions are often in contact with sand at beaches and play areas.
  • compositions In addition to being convenient for the user the compositions must contain adequate solvent to hold the necessary amount of UV-filter. Need continues to exist for compositions which simultaneously have a low or zero content of preservatives, while exhibiting an optimum stability which is maintained throughout the time of storage and ultimate use of the products. Finally, in instances where a particularly high and lasting protection is desired, as for children's skin or for sensitive skin, it is also preferable to employ compositions which exhibit good water resistance and which thus retain a very good photo protective power even after coming into contact with water.
  • sunscreen formulations comprising dimethicone derivatives, wherein from about 75% to about 100% of an SPF rating of the composition is retained after immersion into water for 80 minutes. Corresponding formulation without dimethicone derivatives perform poorly with respect to water resistance.
  • compositions are oil-in-water emulsions.
  • one of the disadvantages of traditional oil-in-water emulsions is that they very easily lose their effectiveness with respect to UV protection as soon as they come into contact with water; this because the screening agents which they contain in their aqueous phase are removed by the water, during bathing in the sea or in swimming pools, for example, or, alternatively, under the shower or when playing water sports, and the overall photoprotective power of these compositions thus is greatly reduced.
  • sunscreen compositions which are solvent solutions with a low water content rather than oil-in-water emulsions would be advantageous.
  • film forming polymers or water proofing agents are added to sunscreen compositions to enhance resistance to water in vivo.
  • sunscreen compositions to enhance resistance to water in vivo.
  • 2011/100275 describes a sunscreen composition formulated as a spray
  • Film forming polymers are however expensive additives and generally it is desirable to reduce the amount of additives in cosmetic compositions such as sunscreen agents.
  • sunscreen compositions which have a high SPF rating and simultaneously maintain a high water resistance, are non-greasy and easily applicable, while comprising reduced amount of additives, such as film forming polymers would be advantageous.
  • an object of the present invention relates to the provision of improved or alternative sunscreen compositions.
  • one aspect of the invention relates to a sunscreen composition comprising at least one sunscreen agent, at least one film forming polymer, and at least one solvent, wherein said film forming polymer is present in an amount of less than 2.0 %(w/w).
  • Another aspect of the present invention relates to a process for the manufacture of a sunscreen composition comprising the steps of
  • step i) providing at least one solvent, at least one film forming polymer in an amount of less than 2.0 %(w/w), and at least one sunscreen agent, ii) admixing the components of step i) to provide a sunscreen
  • sunscreen composition or photoprotective composition is to be understood as a liquid composition comprising agents that reduces the amount of UV radiation being absorbed by the skin, when said sunscreen composition is applied to the skin.
  • a sunscreen composition may either absorb or block the UV rays.
  • UV radiation may include UVA and UVB radiation.
  • Sunscreen compositions may be formulated as solutions, emulsions, milks or oils, and may be applied to the skin by the means of sprays, creams, or lotions.
  • sunscreen agent is any cosmetologically approved agent capable of adsorbing or blocking UV radiation, such as UVA and/or UVB radiation.
  • Sunscreen agents that absorb UV radiation are also referred to as UV filters, UVA, UVB or broad spectrum filters.
  • sunscreen agents are often organic compounds or molecules, which absorb light in the UV region, the UV region being at wavelengths from 290 to 400 nanometers.
  • Sunscreen agents that block the UV rays may include substances that leave a white coating on the skin, such as certain metal oxides including for example titanium oxide or other white substances.
  • film forming polymer also sometimes referred to as a "waterproofing agent” is a polymer capable of forming a film on e.g. skin as the carrier or solvent that it is dissolved in evaporates.
  • a film forming polymer may be a uniform homo-polymer or a co-polymer, such as for example a block-copolymer.
  • the polymer should be suitable for use in cosmetic products and may preferably be cosmetologically approved.
  • co-polymer relates to a polymer formed when two (or more) different types of monomer are linked in the same polymer chain, as opposed to a homo-polymer where only one monomer is used.
  • solvent also sometimes referred to as a carrier, is any liquid capable of dissolving the components of the sunscreen composition.
  • a solvent may be a mixture of different solvents or it may be a single solvent.
  • the solvent should be suitable for use in cosmetics and may preferably be cosmetologically approved.
  • alcohol refers to an organic compound in which a hydroxyl group (-OH) is attached to a saturated carbon atom.
  • Alcohols have the general formula ROH, where R may be a lower-aliphatic or cyclic carbon chain and may include aromatic rings. Alcohols are further classified as primary, secondary or tertiary, according to the position of the hydroxyl group on the lower-aliphatic carbon chain. Alcohols may also be classified by the number of hydroxyl groups present in the molecule; for example, a compound with two hydroxyl groups (a diol), and with three hydroxyl groups (a triol). The alcohol may comprise a denaturant.
  • Alcohol Denaturant relates to ethyl alcohol that is denatured with one or more denaturing agents.
  • One such denaturing agent may be Denatonium Benzoate.
  • a “solution” according to the present invention consists of a solvent and a range of ingredients which are all entirely dissolved in said solvent.
  • a solution does not comprise any solid dispersed material, i.e. it is not a dispersion.
  • a solution does not comprise other liquid immiscible components which may or may not form vesicles that are dispersed in said solution, i.e. the solution is not an emulsion.
  • an “anhydrous" composition means a composition which is essentially free of water. Essentially free of water entails that no water is added to a composition, however minor amounts of water may be present since other components added to the composition may comprise small amount of water.
  • anhydrous composition means a composition entirely free of water.
  • MED minimal erythema dose
  • SPF Sun protection factor
  • MEDp minimum erythemal dose on protected skin
  • MED U minimum erythemal dose on unprotected skin
  • the Sun Protection Factor value on an individual subject may be determined as the ratio of the minimum erythemal dose on protected skin (MED P ) to the minimum erythemal dose on unprotected skin (MED U ) of the same subject.
  • the term “static sun protection factor”, (SPF S ), relates to the sun protection factor before water immersion
  • the term “wet sun protection factor” (SPFw) refers to the sun protection factor after water immersion.
  • the static and wet SPF values are determined according to the current published International Sun Protection Factor (SPF) Test Method (I-SPF-TM) as defined in 2006 by COLIPA (CTFA SA - JCIA - CFTA US) as well as international standard ISO 24444: 2010(E).
  • thickening agent is any agent which is capable of increasing the viscosity of a cosmetic composition such as for example a sunscreen composition.
  • the agent may preferably be cosmetologically approved.
  • a first aspect of the present invention is a sunscreen composition
  • a sunscreen composition comprising at least one sunscreen agent, at least one film forming polymer, and at least one solvent, wherein said film forming polymer is present in an amount of less than 2.0 %(w/w).
  • the sunscreen composition may preferably be a sprayable sunscreen composition.
  • sprayable or “sprayable sunscreen composition” relates to a composition which is capable of being formulated and dispensed as a spray.
  • a further preferred quality to a sprayable composition is that said composition when dispensed using a spray dispenser, preferably a spray dispenser not comprising a propellant, is dispensed in a way which allows sufficient and even distribution of the composition onto the skin.
  • a sprayable sunscreen composition should preferably have a viscosity which allows it to form an aerosol upon dispensing it as a spray, and it should preferably be dispensable in a volume which allows for sufficient coverage of the skin.
  • the present sunscreen composition is formulated as a spray.
  • the viscosity of said sunscreen composition may be below 120 cP at 25 °C, such as below 110 cP at 25 °C, 100 cP at 25 °C, 80 cP at 25 °C,
  • the sunscreen composition may thus have a viscosity in the range of 1-120 cP at 25 °C, such as in the range of 1-110 cP at 25 °C, 1-100 cP at 25 °C, 1-80 cP at 25 °C, 1-60 cP at 25 °C, 1-40 cP at 25 °C, 1-30 cP at 25 °C, 1-20 cP at 25 °C, 1-15 cP at 25 °C, 1-14 cP at 25 °C, 2-13 cP at 25 °C, 3-12 cP at 25 °C,
  • the present sunscreen composition comprises a film forming polymer, which provides for better water resistance of the composition.
  • a film forming polymer which provides for better water resistance of the composition.
  • polyvinylpyrrolidone PVP
  • acrylates acrylamides
  • the film forming polymer is selected from the group consisting of acrylate/octylacrylamide copolymer, acrylates copolymer, acrylates/Ci2-22 alkyl methacrylate copolymer, butylated PVP), VA/butyl maleate/isobornyl acrylate copolymer vinyl caprolactam/VP/dimethylaminoethyl
  • the film forming polymer would provide excellent water resistance of the present sunscreen compositions even at very low weight percentages.
  • the film forming polymer may preferably be present in
  • the sunscreen composition in an amount of less than 1.8%(w/w), such as less than 1.6%(w/w), less than 1.4%(w/w), less than 1.2%(w/w), less than
  • the film forming polymer is present in an amount in the range of 0.1-2.0%(w/w), such as in the range of
  • said sunscreen composition comprises water in an amount of 0-2%(w/w), such as 0-l%(w/w), such as 0- 0.8%(w/w), 0-0.6%(w/w), 0-0.4%(w/w), 0-0.2%(w/w), 0-0.1%(w/w), 0- 0.05%(w/w), such as 0-0.01%(w/w).
  • the composition is essentially anhydrous and most preferably the composition is anhydrous.
  • the solvent of the present invention may preferably be an alcohol.
  • Said alcohol may be a mono alcohol having 2-8 carbon atoms, such as 2-4 carbon atoms.
  • the alcohol is selected from the group consisting of ethanol, 1- propanol, 2-propanol, ethyleneglycol, 1-butanol, 2-butanol or any combination thereof. Ethanol is particularly preferred.
  • the alcohol may comprise a denaturant, particularly when the alcohol is ethanol.
  • the solvent content may preferably be in the range of 10-90%(w/w), such as in the range of 15-85%(w/w), 20-80%(w/w), 25-70%(w/w), 28-65%(w/w), 30-60%(w/w), 30-50%(w/w), such as in the range of 30-40%(w/w) or in the range of 20-30%(w/w).
  • the sunscreen composition according to the present invention is a solution.
  • the components of the present compositions are preferably dissolved entirely in the solvent without forming for example emulsions or milks, and even more preferably the sunscreen composition does not comprise emulsifiers.
  • the sunscreen composition comprises one or more sunscreen agents, which provide the adsorption or blocking of the UV radiation, before it reaches the skin.
  • the sunscreen agent may be selected from the group consisting of Avobenzone, Cinoxate, Dioxybenzone, Homosalate, Menthyl anthranilate, Octocrylene, Octyl methoxycinnamate, Octyl salicylate, Oxybenzone, Padimate O,
  • Phenylbenzimidazole sulfonic acid Sulisobenzone, Titanium dioxide, Trolamine salicylate, Zinc oxide, Benzophenone-3 , Ethylhexyl Methoxycinnamate,
  • dibenzimidazole tetrasulfonate bis-ethylhexyloxyphenol methoxyphenol triazine
  • methylene bisbenzotriazolyl tetramethylbutylphenol bisethylhexyloxyphenol methoxyphenyl triazine and any combination thereof.
  • the at least one sunscreen agent is selected from the group consisting of Homosalate, Octocrylene, Ethylhexyl Methoxycinnamate, Butyl Methoxydibenzoylmethane (BMBM), Diethylamino Hydroxybenzoyl Hexyl Benzoate, diethylhexyl butamido triazone, ethylhexyl salicylate or any combination thereof.
  • BMBM Butyl Methoxydibenzoylmethane
  • Diethylamino Hydroxybenzoyl Hexyl Benzoate diethylhexyl butamido triazone
  • ethylhexyl salicylate or any combination thereof.
  • Even more preferred is a composition comprising Homosalate, Octocrylene, Ethylhexyl Methoxycinnamate, Butyl
  • BMBM Methoxydibenzoylmethane
  • Diethylamino Hydroxybenzoyl Hexyl Benzoate Diethylhexyl butamido triazone.
  • the amount of each individual sunscreen agent used in a given sunscreen composition is determined by the desired SPF value and regulatory limitations for the percentage (w/w) of sunscreen agent allowed in sunscreen compositions for a given jurisdiction.
  • To achieve broad range UV protection it may advantageous to add both UVA, UVB and broad range UV filters.
  • further amounts of a different sunscreen agent may be added or preferably the SPF may be boosted by other means, such as described herein. Therefore, in preferred embodiments
  • Diethylamino Hydroxybenzoyl Hexyl Benzoate is used in concentrations of at the most 10 %(w/w), e.g. in the range of 0.1-10%(w/w), such as in the range of 3- 10%(w/w), e.g. in the range 5-10%(w/w), such as in the range of 7-10%(w/w), and/or Ethylhexyl Methoxycinnamate is used in concentrations of at the most 2%(w/w), e.g. in the range of 0.01-2%(w/w), such as in the range of 0.01- l%(w/w), e.g.
  • Octocrylene is used in concentrations of at the most 10%(w/w), e.g. in the range of 0.1-10%(w/w), such as in the range of 0.5-8%(w/w), e.g. in the range l-6%(w/w), such as in the range of 3-5%(w/w), e.g. in the range 6-10%(w/w), such as in the range of 8- 10%(w/w) and/or Butyl Methoxydibenzoylmethane (BMBM) is used in concentrations of at the most 10%(w/w), e.g. in the range of 0.1-10%(w/w), such as in the range of 0.5-8%(w/w), e.g. in the range l-6%(w/w), such as in the range of 3-5%(w/w), e.g. in the range 6-10%(w/w), such as in the range of 8- 10%(w/w) and/or Butyl Methoxydi
  • concentrations of at the most 5%(w/w), such as in the range of 0.5-5%(w/w), e.g. in the range 3-5%(w/w), such as in the range of 4-5%(w/w) and/or homosalate is used in concentrations of at the most 10%(w/w), e.g. in the range of 0.1-10%(w/w), such as in the range of 0.5-8%(w/w), e.g.
  • Diethylamino Hydroxybenzoyl Hexyl Benzoate is used in concentrations about 10%(w/w), and optionally Ethylhexyl
  • Methoxycinnamate is used in concentrations of 0.01 (w/w)
  • Octocrylene is used in concentrations of about 10%(w/w)
  • Butyl Methoxydibenzoylmethane (BMBM) is used in concentrations of about 5%(w/w) and homosalate is used in concentrations of about 10%(w/w)
  • diethylhexyl butamido triazone is used in concentrations of about 4.5%(w/w)
  • ethylhexyl salicylate is used in
  • the sunscreen composition may comprise several sunscreen agents to achieve the desired SPF value.
  • the composition comprises at least 2 sunscreen agents, such as 3 sunscreen agents, e.g. 4 sunscreen agents, such as 5 sunscreen agents, e.g. 6 sunscreen agents, such as 7 sunscreen agents.
  • the present composition comprises butyloctyl salicylate.
  • Said salicylate may be present in the composition in an amount in the range of 0.1-15%(w/w), such as 0.1-10%(w/w), 0.5-10%(w/w), 1.0-10%(w/w), 2-10%(w/w), 3-10%(w/w), 4-10%(w/w), 5-10%(w/w), 6-10%(w/w), 7- 10%(w/w), 8-10%(w/w), 9-10%(w/w), 9.5-10%(w/w), such as about 10%(w/w).
  • Butyloctyl salicylate may function as SPF booster and as co-solvent.
  • Silicone derivatives are used as emollients in for example sunscreen compositions and they also provide for improved skin feel. Since silicone derivatives may become subject of regulatory limitations "silicone alternatives" are also available, which provide similar effects to silicone derivatives but are mostly non-silicone compounds or compound mixtures derived from natural sources.
  • the composition further comprises a siloxane or a silane or silicone alternative, such as a siloxane, silane or silicone alternative selected from the group consisting of Ci 3 -i 6 isoparaffin, Ci 2 -i 4 isoparaffin, Ci 3 _i 5 Alkane,
  • siloxane, silane or silicone alternative may be present in an amount in the range of 0.1-20%(w/w), such as in the range of 0.5-15%(w/w), e.g. in the range of l-10%(w/w), such as in the range of 2-7%(w/w), e.g.
  • the present sunscreen composition may advantageously comprise an alkoxylated alcohol, which may serve as an emollient and/or co-solvent.
  • the alkoxylated alcohol may preferably a long chain C 11 -C15 aliphatic alkoxylated alcohol and may be selected from the group consisting of PPG-11 stearyl ether, PPG-15 Stearyl ether, or any combination thereof.
  • the alkoxylated alcohol may be added in an amount in the range of 0.1-20%(w/w), such as in the range of 0.5-15%(w/w), e.g. in the range of l-10%(w/w), such as in the range of 2-7%(w/w), e.g. in the range of 5-7%(w/w).
  • the present composition may further comprise an ester, which may serve as an emollient and/or co-solvent.
  • the ester may preferably be selected from the group consisting of Ethylhexyl Benzoate, Dibutyl Adipate, Neopentyl Glycol
  • the ester may be present in an amount which is less 15%(w/w) such as less than
  • 10%(w/w) such as less than than 5%(w/w), such as less than 4%(w/w), less than 3%(w/w), less than 2%(w/w), less than l%(w/w), less than 0.5%(w/w), less than 0.2%(w/w), such as less than 0.1%(w/w).
  • the composition may comprise a thickening agent.
  • Said thickening agent may preferably be a polysaccharide thickening agent. It may preferably be a cellulosic material, and may preferably be selected from the group consisting of cellulose, carboxymethyl hydroxyethylcellulose, hydroxypropyl methylcellulose, methyl hydroxyethylcellulose, microcrystalline cellulose, sodium cellulose sulphate, hydroxyethylcellulose, hydroxypropylcellulose, and any mixtures thereof.
  • the wet sun protection factor of the composition is at least 90% of the static sun protection factor, such as at least 95%, 100%, 105%, 110%, 115%, such as at least 120%, when the composition is contacted with water, particularly after the composition has been immersed in water in vivo for 80 minutes.
  • the composition having a static sun protection factor after the composition has been applied to the skin of a human the sun protection factor of the composition is capable of being increased to a higher wet sun protection factor when the composition is contacted with water, particularly after the composition has been immersed in water in vivo for 80 minutes.
  • a preferred sunscreen composition is a composition wherein the wet sun protection factor is increased by at least 5% relative to the static sun protection factor, such as increased by at least 10% relative to the static sun protection factor, e.g.
  • the water resistance of a sunscreen composition may be measured according to internationally or regionally approved standards such as for example the
  • a sunscreen having a particularly high water resistance according to the regional or international standard may be designated by a "very water resistance” (VWR) value.
  • Very Water Resistance is measured in vivo after a test subject has been immersed in water for a total of 80 minutes i.e. 4 times 20 minutes with 15 min drying time in between.
  • the present invention is a composition wherein the Very Water Resistance value of said composition is above 50, such as above 60, above 70, above 80, such as above 85, above 90, above 95, above 100, above 105, such as above 110.
  • a highly preferred embodiment of the present invention is to provide a sunscreen composition with a high SPF value.
  • the present invention relates to a sunscreen composition wherein the sunscreen protection factor of said composition is at least 40, such as at least 42, at least 44, at least 46, at least 48, at least 50, at least 51, at least 52, at least 53, at least 54, such as at least 55.
  • the sunscreen composition is preferably provided that achieves a high SPF value and a high water resistance while using a minimal amount of sunscreen agents.
  • the composition comprises no more than 7 sunscreen agents and wherein the sun protection factor is at least 30, such as at least 32, at least 34, at least 36, at least 38, at least 40, at least 42, at least 44, at least 46, at least 48, at least 50, at least 52, at least 53, at least 54, such as at least 55, such as no more than 6 sunscreen agents and wherein the sun protection factor is at least 30, such as at least 32, at least 34, at least 36, at least 38, at least 40, at least 42, at least 44, at least 46, at least 48, at least 50, at least 52, at least 53, at least 54, such as at least 55.
  • the sun protection factor is at least 30, such as at least 32, at least 34, at least 36, at least 38, at least 40, at least 42, at least 44, at least 46, at least 48, at least 50, at least 52, at least 53, at least 54, such as at least 55.
  • UVA protection may either be expressed via the so-called COLIPA ratio or via the Boots star rating system, the guidelines for both of these rating systems being described in the below examples.
  • the present sunscreen compositions may preferably have a COLIPA ratio below 3, such as below 2, below 1.8.
  • the present sunscreen composition has a boots star rating of at least 4 stars.
  • a preferred embodiment of the present invention is a sunscreen composition wherein the SPF value of said composition 10 hours after application in vivo is at least 60%, such as at least 65%, at least 70%, at least 75%, such as at least 78% of the SPF value of said sunscreen composition 15 minutes after application in vivo.
  • SPF value is the static SPF value.
  • Another aspect of the present invention is a process for the manufacture of a sunscreen composition comprising the steps of
  • step i) providing at least one solvent, at least one film forming polymer in an amount of less than 2.0 %(w/w), and at least one sunscreen agent, ii) admixing the components of step i) to provide a sunscreen
  • the mixture or composition is not heated during the process and the temperature is in the range of 0-60 °C, such as in the range of 5-55 °C, 15-50 °C, 20-50 °C, 30-45 °C, such as about 40 °C.
  • no water is added to the composition during said process, and even more preferably the components provided in step i) are admixed in the order provided in step i). Further additives as described herein may be added in step i). Each component added is dissolved under stirring before the next component is added. Stirring time may vary from 1- 25 minutes. All the embodiments described for the aspect relating to a sunscreen composition may naturally also apply to the sunscreen composition described for the present method of manufacturing.
  • Example 1 Sunscreen compositions and manufacture thereof
  • compositions were manufactured by addition of the listed components in the order they are listed under stirring using a Silverson L4RT high shear mixer.
  • wet SPF as measured in vivo is the SPF value measured after application of sunscreen and subsequent immersion of the test individual in water for 80 minutes.
  • the immersion in water for 80 minutes is divided into 4
  • the very water resistance value (in percentage) is calculated as:
  • VWR 100 x SPF W /SPF S where the lower limits of the confidence intervals (95% CI) is used for SPF W and SPF S based on statistics performed on the data from 12 test subjects.
  • compositions A and B are compositions A and B.
  • compositions of the present invention retain a very high water resistance even with very low levels of film forming polymer present, which justifies the label "very water resistant" according to the recommendations in the abovementioned guidelines.
  • the requirement for this label is a water resistance of 50% or more.
  • the protection against UVA radiation may be determined by the COLIPA ratio as defined in the COLIPA guideline (in vitro method for the determination of the UVA protection factor and "critical wavelength" values of sunscreen products".
  • COLIPA Ratio SPFiabei/UVA-PF where UVA-PF is the actual "SPF" obtained for UVA irradiation measured in vitro according to the guidelines.
  • the present compositions A and B were tested and displayed a COLIPA ratio of 1.6 and 1.7 respectively, which fulfils the
  • UVA protection was also determined by the Boots star rating system
  • compositions A and B fulfils these criteria.
  • the viscosity of the present sunscreen compositions must be within certain limits for the compositions to remain sprayable.
  • the viscosity of composition A was investigated along with compositions having more thickening agent (solvent amounts being adjusted accordingly).
  • the viscosities were measured at 25 °C at 60 rpm using a Brookfield LVDV-II + P viscometer with a small sample adapter and Spindle S18.
  • HPC hydroxypropylcellulose
  • sunscreen products and the claims made relating thereto (notified under document number C(2006) 4089) (Text with EEA relevance) (2006/647/EC); Official Journal of the European Union, L 265/3

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  • General Health & Medical Sciences (AREA)
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Abstract

Un aspect de l'invention concerne une composition d'écran solaire comprenant au moins un agent de protection solaire, au moins un polymère filmogène, et au moins un solvant, dans lequel ledit polymère filmogène est présent en une quantité inférieure à 2,0% (w/w). Un autre aspect de la présente invention concerne un procédé pour la fabrication d'une composition d'écran solaire comprenant les étapes consistant à i) la fourniture d'au moins un solvant, au moins un polymère filmogène en une quantité inférieure à 2,0% (w/w) , et au moins un agent de protection solaire, ii) à mélanger les composants de l'étape i) afin de produire une composition d'écran solaire.
EP13747962.2A 2012-07-26 2013-07-25 Composition d'écran solaire, resistant a l'eau haute protection améliorée Withdrawn EP2877148A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA201200477 2012-07-26
PCT/DK2013/050251 WO2014015880A2 (fr) 2012-07-26 2013-07-25 Composition d'écran solaire haute protection améliorée

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US (1) US20150202131A1 (fr)
EP (1) EP2877148A2 (fr)
KR (1) KR20150040958A (fr)
CN (1) CN104661638A (fr)
BR (1) BR112015001652A2 (fr)
CA (1) CA2879475A1 (fr)
IN (1) IN2015DN00518A (fr)
RU (1) RU2015105526A (fr)
WO (1) WO2014015880A2 (fr)

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DE102014206219A1 (de) * 2014-04-01 2015-10-01 Beiersdorf Ag Zellulose-haltige kosmetische Zubereitung mit erhöhter Hautbefeuchtung
DE102015208855A1 (de) * 2015-05-13 2016-11-17 Beiersdorf Ag Octocrylenfreies Sonnenschutzmittel mit Diethylhexylbutanidotriazon
DE102015208872A1 (de) * 2015-05-13 2016-11-17 Beiersdorf Ag Octocrylenfreies Sonnenschutzmittel mit Diethylaminohydroxybenzoylhexylbenzoat
CN106046976B (zh) * 2016-05-25 2018-03-02 河南鑫瑞达节能建材科技有限公司 一种耐紫外线负离子装饰板的制备工艺
CN107638343B (zh) * 2017-09-19 2019-11-15 澳宝化妆品（惠州）有限公司 一种含植物抗敏组分的防晒喷雾组合物
CN107638307A (zh) * 2017-09-19 2018-01-30 澳宝化妆品（惠州）有限公司 一种防晒喷雾组合物
CN108852875A (zh) * 2018-08-23 2018-11-23 无限极（中国）有限公司 一种防晒组合物及其制备的化妆品
FR3085271B1 (fr) * 2018-08-30 2021-10-29 Naos Inst Of Life Science Composition lavante et de protection solaire a haute remanence
CN115003388A (zh) * 2020-01-23 2022-09-02 陶氏环球技术有限责任公司 基于硫酸化结晶纤维素spf增效剂的水性防晒调配物
LU101670B1 (en) * 2020-03-09 2021-09-10 Soc De Recherche Cosmetique Sarl Sun protection topical composition
AU2022348925A1 (en) * 2021-09-23 2024-04-04 Edgewell Personal Care Brands, Llc Sunscreen composition with crystalline organic sunscreen filters
KR102639495B1 (ko) * 2023-11-28 2024-02-22 주식회사 부쉬맨 방수 썬크림 조성물

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IN2015DN00518A (fr) 2015-06-26
BR112015001652A2 (pt) 2017-07-04
WO2014015880A3 (fr) 2014-07-17
CN104661638A (zh) 2015-05-27
US20150202131A1 (en) 2015-07-23
CA2879475A1 (fr) 2014-01-30
RU2015105526A (ru) 2016-09-20
KR20150040958A (ko) 2015-04-15
WO2014015880A2 (fr) 2014-01-30

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